Albers Mark J, Bok Robert, Chen Albert P, Cunningham Charles H, Zierhut Matt L, Zhang Vickie Yi, Kohler Susan J, Tropp James, Hurd Ralph E, Yen Yi-Fen, Nelson Sarah J, Vigneron Daniel B, Kurhanewicz John
Department of Bioengineering, University of California San Francisco, San Francisco, California 94158-2330, USA.
Cancer Res. 2008 Oct 15;68(20):8607-15. doi: 10.1158/0008-5472.CAN-08-0749.
An extraordinary new technique using hyperpolarized (13)C-labeled pyruvate and taking advantage of increased glycolysis in cancer has the potential to improve the way magnetic resonance imaging is used for detection and characterization of prostate cancer. The aim of this study was to quantify, for the first time, differences in hyperpolarized [1-(13)C] pyruvate and its metabolic products between the various histologic grades of prostate cancer using the transgenic adenocarcinoma of mouse prostate (TRAMP) model. Fast spectroscopic imaging techniques were used to image lactate, alanine, and total hyperpolarized carbon (THC = lactate + pyruvate + alanine) from the entire abdomen of normal mice and TRAMP mice with low- and high-grade prostate tumors in 14 s. Within 1 week, the mice were dissected and the tumors were histologically analyzed. Hyperpolarized lactate SNR levels significantly increased (P < 0.05) with cancer development and progression (41 +/- 11, 74 +/- 17, and 154 +/- 24 in normal prostates, low-grade primary tumors, and high-grade primary tumors, respectively) and had a correlation coefficient of 0.95 with the histologic grade. In addition, there was minimal overlap in the lactate levels between the three groups with only one of the seven normal prostates overlapping with the low-grade primary tumors. The amount of THC, a possible measure of substrate uptake, and hyperpolarized alanine also increased with tumor grade but showed more overlap between the groups. In summary, elevated hyperpolarized lactate and potentially THC and alanine are noninvasive biomarkers of prostate cancer presence and histologic grade that could be used in future three-dimensional (13)C spectroscopic imaging studies of prostate cancer patients.
一种使用超极化(13)C标记丙酮酸并利用癌症中糖酵解增加的非凡新技术,有可能改善磁共振成像用于前列腺癌检测和特征描述的方式。本研究的目的是首次使用小鼠前列腺转基因腺癌(TRAMP)模型,量化前列腺癌不同组织学分级之间超极化[1-(13)C]丙酮酸及其代谢产物的差异。使用快速光谱成像技术在14秒内对正常小鼠以及患有低级别和高级别前列腺肿瘤的TRAMP小鼠的整个腹部进行乳酸、丙氨酸和总超极化碳(THC = 乳酸 + 丙酮酸 + 丙氨酸)成像。在1周内,解剖小鼠并对肿瘤进行组织学分析。随着癌症的发展和进展,超极化乳酸的信噪比水平显著增加(P < 0.05)(正常前列腺、低级别原发性肿瘤和高级别原发性肿瘤中的信噪比分别为41 +/- 11、74 +/- 17和154 +/- 24),并且与组织学分级的相关系数为0.95。此外,三组之间乳酸水平的重叠最小,七个正常前列腺中只有一个与低级别原发性肿瘤重叠。THC(一种可能的底物摄取指标)和超极化丙氨酸的量也随肿瘤分级增加,但组间显示出更多重叠。总之,升高的超极化乳酸以及可能的THC和丙氨酸是前列腺癌存在和组织学分级的非侵入性生物标志物,可用于未来对前列腺癌患者进行的三维(13)C光谱成像研究。